Bile acid profiles in neonatal intrahepatic cholestasis caused by citrin deficiency

Clin Chim Acta. 2017 Dec:475:28-35. doi: 10.1016/j.cca.2017.10.005. Epub 2017 Oct 4.

Abstract

Background: Neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) is characterized by conjugated hyperbilirubinemia and increased plasma bile acid concentrations. However, the underlying mechanisms remain unclear. We established a liquid chromatography tandem mass spectrometry (LC-MS/MS) method for simultaneously quantifying plasma bile acids and examined bile acid profiles in NICCD infants.

Methods: We measured 15 bile acids within 15min and found a wide linear range for individual bile acids.

Results: The within-run and run-to-run CV of all bile acids was 1.2-10.9% and 3.1-10.8%, respectively, with a mean recovery of 90.5-112.6%. Compared to infants with citrullinemia without mutations in SLC25A13 (non-NICCD), NICCD infants showed increased plasma total bile acid concentrations (mean: 201 vs. 42μM, p<0.001), with a distinct bile acid profile characterized by increased conjugated primary bile acid concentrations. The calculated ratios, including primary/secondary bile acid (714 vs. 235, p<0.05) and conjugated/free bile acid (371 vs. 125, p<0.05) ratios, were higher in NICCD infants. The area under receiver operating characteristic curve for conjugated/free bile acid ratio to identify infants with NICCD was 0.871 (95% confidence interval, 0.713-1.0).

Conclusions: Together, our findings indicated plasma bile acid profile as a potential noninvasive diagnostic biomarker for NICCD.

Keywords: Bile acid profile; Cholestasis; Citrin; Citrullinemia.

MeSH terms

  • Bile Acids and Salts / blood*
  • Bile Acids and Salts / chemistry
  • Biomarkers / blood
  • Biomarkers / chemistry
  • Case-Control Studies
  • Cholestasis, Intrahepatic / blood
  • Cholestasis, Intrahepatic / diagnosis*
  • Citrullinemia / blood
  • Citrullinemia / diagnosis*
  • Female
  • Gene Expression
  • Humans
  • Infant
  • Infant, Newborn
  • Infant, Newborn, Diseases / blood
  • Infant, Newborn, Diseases / diagnosis*
  • Male
  • Mitochondrial Membrane Transport Proteins / deficiency
  • Mitochondrial Membrane Transport Proteins / genetics*
  • Mutation

Substances

  • Bile Acids and Salts
  • Biomarkers
  • Mitochondrial Membrane Transport Proteins
  • SLC25A13 protein, human

Supplementary concepts

  • Adult-onset citrullinemia type 2
  • Neonatal-onset citrullinemia type 2